IP Library Granted Patent US 9,675,676
Granted Patent B2
US 9,675,676 · App. 15/043,445 · Granted Jun 13, 2017

Factor IX polypeptides and methods of use thereof

Inventors: Glenn Pierce (Cambridge, MA); Samantha Truex (Sudbury, MA); Robert T. Peters (Needham, MA); Haiyan Jiang (Belmont, MA)
Assignee: BIOVERATIV THERAPEUTICS INC.
A61K38/4846A61K9/0019A61K38/38A61K39/395A61K39/3955A61K39/39533A61K47/48284C07K14/76C07K16/18C12N9/644C12N9/96C12Y304/21022C07K2317/21C07K2317/90C07K2317/94C07K2319/30C07K2319/31C07K2319/33
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Quick Facts
Patent No.
US 9,675,676
App. No.
15/043,445
Granted
Jun 13, 2017
Kind
B2
Abstract

The present invention provides methods of administering Factor IX; methods of administering chimeric and hybrid polypeptides comprising Factor IX; chimeric and hybrid polypeptides comprising Factor IX; polynucleotides encoding such chimeric and hybrid polypeptides; cells comprising such polynucleotides; and methods of producing such chimeric and hybrid polypeptides using such cells.

Claims (30)

1. A method of treating hemophilia B in a human subject in need thereof, comprising intravenously administering to the subject multiple doses of about 100 IU/kg to about 150 IU/kg of a chimeric Factor IX (“FIX”) polypeptide at a dosing interval of about 19 days to about 40 days between two doses, wherein the chimeric FIX polypeptide comprises FIX and an FcRn binding partner (FcRn BP), which comprises Fe or albumin, and wherein the administration maintains the plasma FIX activity of the subject above 1 IU/dL between the dosing interval.

2. The method of claim 1 , wherein each of the multiple doses is 100 IU/kg.

3. The method of claim 1 , wherein the dosing interval is 19 days, 20 days, 21 days, 22 days, 23 days, 24 days, 25 days, 26 days, 27 days, 28 days, 29 days, 30 days, 31 days, 32 days, 33 days, 34 days, 35 days, 36 days, 37 days, 38 days, 39 days, or 40 days.

4. The method of claim 1 , wherein the FcRn BP comprises albumin.

5. The method of claim 1 , wherein the FcRn BP comprises Fc.

6. The method of claim 1 , wherein the FIX is at least 95% identical to amino acids 1 to 415 of SEQ ID NO:2.

7. The method of claim 1 , wherein the chimeric FIX polypeptide further comprises a linker joining the FIX and the FcRn BP.

8. The method of claim 2 , wherein the chimeric FIX polypeptide further comprises a linker joining the FIX and the FcRn BP.

9. The method of claim 3 , wherein the chimeric FIX polypeptide further comprises a linker joining the FIX and the FcRn BP.

10. The method of claim 4 , wherein chimeric FIX polypeptide further comprises a linker joining the FIX and the FcRn BP.

11. The method of claim 1 , wherein the plasma level of the FIX polypeptide reaches a trough of at least 5 IU/dl after six days after each administration.

12. The method of claim 2 , wherein the plasma level of the FIX polypeptide reaches a trough of at least 5 IU/dl after six days after each administration.

13. The method of claim 1 , wherein the plasma level of the FIX polypeptide reaches a trough of at least 3 IU/dl after six days after each administration.

14. The method of claim 2 , wherein the plasma level of the FIX polypeptide reaches a trough of at least 3 IU/dl after six days after each administration.

15. The method of claim 1 , wherein each of the multiple doses is about 110 IU/kg.

16. The method of claim 1 , wherein each of the multiple doses is about 120 IU/kg.

17. The method of claim 1 , wherein each of the multiple doses is about 130 IU/kg.

18. The method of claim 1 , wherein each of the multiple doses is about 140 IU/kg.

19. The method of claim 1 , wherein each of the multiple doses is about 150 IU/kg.

20. The method of claim 1 , wherein the dosing interval is about 19 days.

21. The method of claim 1 , wherein the dosing interval is about 20 days.

22. The method of claim 1 , wherein the dosing interval is about 21 days.

23. The method of claim 1 , wherein the dosing interval is about 22 days.

24. The method of claim 1 , wherein the dosing interval is about 23 days.

25. The method of claim 1 , wherein the dosing interval is about 24 days.

26. The method of claim 1 , wherein the dosing interval is about 25 days.

27. The method of claim 1 , wherein the dosing interval is about 26 days.

28. The method of claim 1 , wherein the dosing interval is about 27 days.

29. The method of claim 1 , wherein the dosing interval is about 28 days.

30. The method of claim 1 , wherein the dosing interval is about 29 days.

Assignments (3)
CHANGE OF NAME Recorded Feb 16, 2017
From: BIOGEN HEMOPHILIA INC.
To: BIOVERATIV THERAPEUTICS INC.
Reel/Frame 041735/0703 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 26, 2016
From: PIERCE, GLENN; TRUEX, SAMANTHA; PETERS, ROBERT T.; JIANG, HAIYAN
To: BIOGEN IDEC HEMOPHILIA INC.
Reel/Frame 037841/0516 →
CHANGE OF NAME Recorded Feb 24, 2016
From: BIOGEN IDEC HEMOPHILIA INC.
To: BIOGEN HEMOPHILIA INC.
Reel/Frame 037899/0516 →
Continuity (8)
Continuation 13809276
Provisional Application 61363064 · Jul 9, 2010
Provisional Application 61424555 · Dec 17, 2010
Provisional Application 61430819 · Jan 7, 2011
Provisional Application 61438572 · Feb 1, 2011
Provisional Application 61442079 · Feb 11, 2011
Provisional Application 61470951 · Apr 1, 2011
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